Variant #0000540056 (NC_000010.10:g.55582205_55582210del, NM_033056.3:c.5287_5292del (PCDH15))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.55582205_55582210del |
| DNA change (hg38) |
g.53822445_53822450del |
| Published as |
PCDH15(NM_001142763.1):c.5308_5313delGCTCCT (p.A1770_P1771del), PCDH15(NM_001142763.2):c.5308_5313delGCTCCT (p.A1770_P1771del) |
| ISCN |
- |
| DB-ID |
PCDH15_000216 See all 5 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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